# Kapp Surgical Instrument Inc – FDA Inspection, Nov 16, 2018

Source: https://www.keypedia.com/records/fda_inspections/kapp-surgical-instrument-inc/7ca96367-d2c0-4f1f-9863-9f891abe7a19
Source feed: FDA_Inspections

> FDA inspection 1071836 of Kapp Surgical Instrument Inc, November 16, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1071836
- Company Name: Kapp Surgical Instrument Inc
- Inspection Date: 2018-11-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 915420 - 2015-02-24
- FDA Inspection 716182 - 2011-03-22

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

Company: https://www.keypedia.com/companies/kapp-surgical-instrument-inc/73316216-d4d7-4839-a657-d46d97b3fb46

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7